eudamed_udi
Primary ID: 00634782065522
Diagnostix™ (UDI 00634782065522)
Manufactured by American Diagnostic Corporation
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Diagnostix™ - Primary ID 00634782065522
Device Regulatory Overview
The Diagnostix™ (Model/Catalog Number: 700-7IBK) is a medical device manufactured by American Diagnostic Corporation. This product is indexed under FDA Product Code / Category Classification C9006 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 700-7IBK
- Product Code / EMDN
- C9006
- Device Name
- Aneroid Sphygmomanometer
- Database Sync Date
- 2026-08-09 16:47:32
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Diagnostix™?
The registered manufacturer of record for Diagnostix™ is American Diagnostic Corporation.
What is the Primary UDI-DI identifier for Diagnostix™?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00634782065522.
What classification code is assigned to this device?
This device is registered under product classification code C9006.
Similar Classification Devices (C9006)
Other Devices by American Diagnostic Corporation
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